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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Developmental toxicity / teratogenicity

Currently viewing:

Administrative data

Endpoint:
developmental toxicity
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: MIGRATED DATASET. Original reference not translated.

Data source

Reference
Title:
No information
Author:
Gizhlaryan, M.S. et al.: Gig. Sanit. 7, 77-78 (1986)

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
No data
GLP compliance:
no
Remarks:
GLP was not mandatory at the tiem of the study

Test material

Constituent 1
Chemical structure
Reference substance name:
3,4-dichlorobut-1-ene
EC Number:
212-079-0
EC Name:
3,4-dichlorobut-1-ene
Cas Number:
760-23-6
Molecular formula:
C4H6Cl2
IUPAC Name:
3,4-dichlorobut-1-ene
Details on test material:
- Name of test material (as cited in study report): 3,4-dichlorobut-1-ene
- Analytical purity: no data

Test animals

Species:
rat
Strain:
not specified

Administration / exposure

Route of administration:
oral: unspecified
Duration of treatment / exposure:
over the whole gestation period
Frequency of treatment:
daily
Doses / concentrations
Remarks:
Doses / Concentrations:
0.01, 0.1 or 1.0 mg/kg bw
Basis:

Control animals:
yes
Details on study design:
Sex: female

Results and discussion

Results: maternal animals

Maternal developmental toxicity

Details on maternal toxic effects:
Maternal toxic effects:yes

Details on maternal toxic effects:
The dose of 1.0 mg/kg bw led to a significant enhancement of post-implantation losses. 0.1 mg/kg bw caused an increase of pre-implantation losses. Histological examinations revealed changes of placenta.

Results (fetuses)

Details on embryotoxic / teratogenic effects:
Embryotoxic / teratogenic effects:yes

Details on embryotoxic / teratogenic effects:
Histological examinations revealed haemorrhages in embryos (brain and peritoneum) as well as oedema and changes in liver, brain and kidneys. The dose of 0.01 mg/kg bw was tolerated without any damages.

Fetal abnormalities

Abnormalities:
not specified

Overall developmental toxicity

Developmental effects observed:
not specified

Applicant's summary and conclusion